Melittin enhances apoptosis through suppression of IL-6/sIL-6R complex-induced NF-κB and STAT3 activation and Bcl-2 expression for human fibroblast-like synoviocytes in rheumatoid arthritis

被引:114
作者
Kim, Seong-Kyu [1 ,2 ]
Park, Ki-Yeun [2 ]
Yoon, Wern-Chan [1 ]
Park, Sung-Hoon [1 ,2 ]
Park, Kwan-Kyu [3 ]
Yoo, Dae-Hyun [4 ]
Choe, Jung-Yoon [1 ,2 ]
机构
[1] Catholic Univ Daegu, Dept Internal Med, Sch Med, Taegu 705718, South Korea
[2] Catholic Univ Daegu, Dept Internal Med, Arthrtis & Autoimmun Res Ctr, Taegu 705718, South Korea
[3] Catholic Univ Daegu, Dept Pathol, Sch Med, Taegu 705718, South Korea
[4] Hanyang Univ, Hosp Rheumat Dis, Dept Internal Med, Seoul 133791, South Korea
关键词
Melittin; Synoviocyte; Apoptosis; STAT3; NF-kappa B; IL-6; COLLAGEN-INDUCED ARTHRITIS; BEE VENOM; SYNOVIAL FIBROBLASTS; MEDIATOR GENERATION; JOINT DESTRUCTION; CONTROLLED-TRIAL; IL-6; RECEPTOR; INTERLEUKIN-6; CELLS; INFLAMMATION;
D O I
10.1016/j.jbspin.2011.01.004
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective: Resistance to apoptosis of fibroblast-like synoviocytes (FLS) is considered as a major characteristic in RA. This study was designed to identify whether melittin has a pro-apoptotic effect in IL-6/sIL6R-stimulated human FLS by investigating the expression of mitochondrial apoptosis-related genes, nuclear factor-kappa B (NF-kappa B), and signal transducer and activators of transcription (STAT) activation. Methods: Cell viability was determined using a MTT assay after melittin treatment. Expressions of STAT3 and mitochondrial apoptosis-related genes induced by the IL-6/sIL-6R complex were determined by real time-polymerase chain reaction and western blotting. The expression of NF-kappa B p65 following IL-6 stimulation was determined by western blot analysis. The effects of melittin on the expression of apoptosis-related genes and the transcription factors NF-kappa B p65 and STAT3 were assessed in FLS. Apoptosis of FLS was determined by TUNEL-labeling to detect DNA strand breaks and DNA fragmentation assays. Caspase-3 activity was determined by a colorimetric assay. Results: IL-6/sIL-6R induced the activation of the transcription factors, STAT3, NF-kappa B p65 (nucleus), and Bcl-2. Melittin increased the expression of pro-apoptosis-related molecules, namely caspase-3, caspase-9, Apaf-1, and cytosolic cytochrome c, in a dose-dependent manner after treatment with IL-6/sIL-6R. Melittin inhibited STAT3 activation, translocation of NF-kappa B p65 into the nucleus, and expression of anti-apoptotic genes such as Bcl-2 and mitochondrial cytochrome c. Conclusions: The pro-apoptotic effects of melittin likely result from inhibition of the activation of the transcription factors, STAT3 and NF-kappa B p65, and regulation of mitochondrial apoptosis-related genes. Melittin is thus a promising therapeutic option for RA as it induces apoptosis in apoptosis-resistant synoviocytes. (C) 2011 Societe francaise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:471 / 477
页数:7
相关论文
共 32 条
[1]
Interleukin 6 is required for the development of collagen-induced arthritis [J].
Alonzi, T ;
Fattori, E ;
Lazzaro, D ;
Costa, P ;
Probert, L ;
Kollias, G ;
De Benedetti, F ;
Poli, V ;
Ciliberto, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (04) :461-468
[2]
Atiprimod blocks STAT3 phosphorylation and induces apoptosis in multiple myeloma cells [J].
Amit-Vazina, M ;
Shishodia, S ;
Harris, D ;
Van, Q ;
Wang, M ;
Weber, D ;
Alexanian, R ;
Talpaz, M ;
Aggarwal, BB ;
Estrov, Z .
BRITISH JOURNAL OF CANCER, 2005, 93 (01) :70-80
[3]
Interleukin-6: From identification of the cytokine to development of targeted treatments [J].
Assier, Eric ;
Boissier, Marie-Christophe ;
Dayer, Jean-Michel .
JOINT BONE SPINE, 2010, 77 (06) :532-536
[4]
Blockade of interleukin 6 trans signaling suppresses T-cell resistance against apoptosis in chronic intestinal inflammation:: Evidence in Crohn disease and experimental colitis in vivo [J].
Atreya, R ;
Mudter, J ;
Finotto, S ;
Müllberg, J ;
Jostock, T ;
Wirtz, S ;
Schütz, M ;
Bartsch, B ;
Holtmann, M ;
Becker, C ;
Strand, D ;
Czaja, J ;
Schlaak, JF ;
Lehr, HA ;
Autschbach, F ;
Schürmann, G ;
Nishimoto, N ;
Yoshizaki, K ;
Ito, H ;
Kishimoto, T ;
Galle, PR ;
Rose-John, S ;
Neurath, MF .
NATURE MEDICINE, 2000, 6 (05) :583-588
[5]
Apoptosis in rheumatoid arthritis [J].
Baier, A ;
Meineckel, I ;
Gay, S ;
Pap, T .
CURRENT OPINION IN RHEUMATOLOGY, 2003, 15 (03) :274-279
[6]
Control of apoptosis by Rel/NF-κB transcription factors [J].
Barkett, M ;
Gilmore, TD .
ONCOGENE, 1999, 18 (49) :6910-6924
[7]
IL-6 receptor inhibition with tocilizumab improves treatment outcomes in patients with rheumatoid arthritis refractory to anti-tumour necrosis factor biologicals: results from a 24-week multicentre randomised placebo-controlled trial [J].
Emery, P. ;
Keystone, E. ;
Tony, H. P. ;
Cantagrel, A. ;
van Vollenhoven, R. ;
Sanchez, A. ;
Alecock, E. ;
Lee, J. ;
Kremer, J. .
ANNALS OF THE RHEUMATIC DISEASES, 2008, 67 (11) :1516-1523
[8]
Bee venom induces apoptosis through caspase-3 activation in synovial fibroblasts of patients with rheumatoid arthritis [J].
Hong, SJ ;
Rim, GS ;
Yang, HI ;
Yin, CS ;
Koh, HG ;
Jang, MH ;
Kim, CJ ;
Choe, BK ;
Chung, JH .
TOXICON, 2005, 46 (01) :39-45
[9]
Kobayashi T, 2000, ARTHRITIS RHEUM, V43, P1106, DOI 10.1002/1529-0131(200005)43:5<1106::AID-ANR21>3.0.CO
[10]
2-F